CN1951611A - Reduced preparation method for metal nanometer particle using hydroxy ion liquid - Google Patents
Reduced preparation method for metal nanometer particle using hydroxy ion liquid Download PDFInfo
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- CN1951611A CN1951611A CN 200510048415 CN200510048415A CN1951611A CN 1951611 A CN1951611 A CN 1951611A CN 200510048415 CN200510048415 CN 200510048415 CN 200510048415 A CN200510048415 A CN 200510048415A CN 1951611 A CN1951611 A CN 1951611A
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Abstract
The invention relates to a method for using hydroxyl ion liquid to reduce and prepare metal nanometer particles. Wherein, it comprises that: (1), using the cation of hydroxyl group, as N-hydroxyalkyl pyridine ion, N- hydroxyalkyl-N-imidazolidinyl ion, etc, and one acid anion to prepare the ion liquid; (2), using ultrasonic wave to disperse or dissolve metal oxide, metal hydroxide or metal salt into ion liquid; (3), heating the liquid in oil bath; (40, separating the product, washing and vacuum drying. In said invention, the ion liquid can be used as solvent as well as reducer, to avoid inactive foreigner when using catalyst. And the ion liquid is non volatile with better thermal stability. The invention can avoid pollution.
Description
Technical field
The present invention relates to the method that a kind of hydroxy ion liquid reduction prepares metal nanoparticle, belong to the preparation field of nano-powder.
Background technology
It is near the salt that is in a liquid state room temperature that is made of zwitterion that ionic liquid at room temperature (room temperature ionic liquid) is called for short ionic liquid (ionic liquid), it is as a kind of medium of novelty, many characteristics that are different from organic solvent commonly used are arranged: its liquid temperature is interval big, can reach more than 300 ℃; Optionally be dissolved in the inorganic salts that can't dissolve in many organic solvents; There is not significant vapour pressure; Stable, nonflammable, be a kind of green solvent of environmental protection; Therefore ionic liquid is widely used in electrochemistry, catalysis, the organic synthesis.
The existing a large amount of reports of the preparation of nano particle, common liquid phase reduction prepares metallic nano-particle advantage economical and practical, easy production in enormous quantities, but reactions steps complexity, palpus add a large amount of dressing agents, produce a large amount of waste liquids, waste gas, environmental pollution is serious, as the Chinese patent publication number is 1483539,1672836,1680060, and United States Patent (USP) is NO.2005002829, NO.2004131937 etc.Be in the common room temperature ionic liquid, to prepare metal nano material in addition, as the Chinese patent publication number is 1559663A, need to add reducing agent, like this in the ionic liquid with regard to remaining other a large amount of compounds, except that product being had certain influence, catalytic performance that also can remarkable influence ionic liquid doped with nanometer particle, influence the metal nano particle-doped tribological property of ionic liquid, some aspect has limited ion liquid metal nano particle-doped application greatly, and these methods are all complicated, are unfavorable for producing in enormous quantities.
Summary of the invention
The purpose of this invention is to provide a kind of method of utilizing the ionic liquid at room temperature reduction to prepare metal nanoparticle.
The present invention is by the following technical solutions:
The hydroxy ion liquid reduction prepares the method for metal nanoparticle, comprises following step:
(1) makes ionic liquid by cation and a kind of acid radical anion of hydroxy functional groups on a kind of side chain;
(2) metal oxide, metal hydroxides or slaine are dispersed or dissolved in the ionic liquid through ultrasonic;
(3) liquid-phase reaction system that will disperse or dissolve heats under oil bath;
(4) product separates in the system of back to reacting, and separated products is washed and vacuum drying treatment.
The cation of hydroxy functional groups is N-hydroxyalkyl pyridinium ion, N-hydroxyalkyl-N-alkyl imidazole ion or N, N-dihydroxyalkyl imidazol ion on the side chain; Anion is F
-, Cl
-, Br
-, BF
4 -, PF
6 -, N0
3 -, CF
3COO
-, C
3F
7COO
-, CF
3SO
3 -, C
4F
9SO
3 -, (CF
3SO
2)
2N
-, (C
2F
5SO
2)
2N
-, (CF
3SO
2)
3C
-, SbF
6 -, AsF
6 -
Glyoxaline cation is:
Wherein k is the integer of 0-11, and m is the integer of 0-9, and n is the integer of 0-9;
Pyridylium is:
Wherein n is the integer of 0-9;
Metal oxide, metal hydroxides or slaine are IB, IIB, the solid metal oxide of VIIIB, metal hydroxides, slaine except that Zn, Fe, Co compound.
Slaine is sulfate, carbonate, nitrate, oxalates, acetate, iodate, borofluoride, fluorophosphate or halide.
Be 0.5-8h described heat time heating time, and described heating-up temperature is 80 ℃-200 ℃.
The present invention has many significant beneficial effects, its adopts hydroxy ion liquid directly to reduce the preparation metal nanoparticle, ionic liquid is except that as the solvent, also participate in reaction as reducing agent, except that raw material, need not to add other chemical substances in the course of reaction, avoided introducing to the disadvantageous impurity of catalyst, and that ionic liquid at room temperature has is non-volatile, the advantage of Heat stability is good, do not use and discharge a large amount of poisonous and hazardous waste liquids, waste gas in the reaction, so this method is environmental protection, can avoid pollution to environment.In addition, ionic liquid can stop the reunion of nanoparticle as dressing agent, and this method can be metal simple-substance with feedstock conversion basically fully, productive rate height, product purity height.Use certain raw material, suitably control preparation condition, this method can be used for optionally preparing nano particle, nanometer rods, nano wire etc.Preparation technology of the present invention is simple, does not need cost and complex equipment, is suitable for different productions in batches.
Description of drawings
Preparation technology's flow process of Fig. 1 hydroxy ion liquid reduction preparation metal nanoparticle;
The XRD figure of Fig. 2 embodiment 1 preparation Ag nano particle;
The XRD figure of Fig. 3 embodiment 4 preparation Pd nano particles;
The TEM photo of Fig. 4 embodiment 1 preparation Ag nano particle;
The TEM photo of Fig. 5 embodiment 2 preparation Ag nanometer rods;
The TEM photo of Fig. 6 embodiment 3 preparation Ag nano wires;
The TEM photo of Fig. 7 embodiment 4 preparation Pd nanometer rods;
The TEM photo of Fig. 8 embodiment 5 preparation Ag nano particles;
The TEM photo of Fig. 9 embodiment 6 preparation Ag nano particles;
The used instrument of TEM photo is JEM100CX-type transmission electron microscope (Japanese JEOL company), accelerating potential 100kV, and the sample dispersion solvent is a distilled water, drops on the copper mesh of carbon film carrying to detect; The used instrument of XRD analysis is X Pert ProX ray powder diffraction instrument (Dutch Philip company), adopt Cu Ka line excitaton source, λ=0.15405nm, voltage 40kV, electric current 40mA, sample can be powder and places pressing of sample platform groove or sample dispersion to drip on slide in acetone, dries the back and becomes film, directly detects.
Preparation method of ionic liquid is: with 1-alkyl imidazole or imidazoles or pyridine and w-haloalkyl alcohol isothermal reaction certain hour, the halide ion liquid that obtains exchanges with sodium fluoborate through purifying, dry back, obtains the target product ionic liquid at room temperature.
The specific embodiment
Embodiment 1 preparation Ag nanoparticle
(1) ion liquid preparation: get 0.48mol chlorethanol and the 0.32mol methylimidazole 24h that in 80 ℃ of oil baths, refluxes, get the thickness colourless transparent liquid after the reaction, when temperature is reduced to normal temperature, the amplification quantity thermal change is a solid, with ether washing four times, obtain clear crystal 1-ethoxy-3-methylimidazole chlorion liquid, 80 ℃ of dry 48h in vacuum drying oven get dry 1-ethoxy-3-methylimidazole chlorion liquid 25g (0.15mol) and add in the 150mL acetone, add 19g (0.17mol) sodium fluoborate again, stirring at room 24h, suction filtration, filter residue is a waxy solid, uses the acetone washed twice, cleaning solution and filtrate merge, and use anhydrous MgSO
4Dried overnight, 40 ℃ of rotary evaporations go out acetone, and 100 ℃ of oil bath rotary evaporation moisture 2h promptly get pure 1-ethoxy-3-methylimidazole borofluoride ion liquid then.
(2) with 20mg AgBF
4Join 5mL 1-ethoxy-3-methyl imidazolium tetrafluoroborate ([C
2OHmim] BF
4) in the ionic liquid, ultrasonic processing makes its dissolving, stops heating after 2 hours in heating in 100 ℃ of oil baths, with the product centrifugation, wash four times vacuum drying under the normal temperature then with acetone after the cooling, promptly obtain the Ag nanoparticle, average size of products is 25nm, is the face-centered cubic crystal formation.
Embodiment 2 preparation Ag nanometer rods
(1) weighing 0.85g AgNO
3Be dissolved in the 50mL distilled water, dropwise add the 0.5g TGA after the dissolving, mix in the solution of back and produce a large amount of light-yellow precipitate gradually, after TGA dropwises, reaction was carried out 1 hour again, and normal pressure filters, and product washs three times with distilled water, the normal pressure vacuum drying, dry back porphyrize gets the TGA silver powder;
(2) ion liquid preparation: 1-(4 '-hydroxyl) butyl-3-methyl imidazolium tetrafluoroborate ([C
4OHmim] BF
4) the ionic liquid preparation process is with embodiment 1;
(3) 10mg TGA silver is joined 5mL 1-(4 '-hydroxyl) butyl-3-methyl imidazolium tetrafluoroborate ([C
4OHmim] BF
4) in the ionic liquid, ultrasonicly making its dispersion, heating is 4 hours in 160 ℃ of oil baths, and centrifugation goes out product behind the cool to room temperature, and with acetone washing four times, last normal pressure vacuum drying promptly gets the Ag nanometer rods.
Embodiment 3 preparation Ag nano wires
(1) ion liquid preparation: 1-(6 '-hydroxyl) hexyl-3-methyl imidazolium tetrafluoroborate ([C
6OHmim] BF
4) ion liquid preparation process is with embodiment 1;
(2) preparation of TGA silver: with embodiment 2;
(3) claim 10mg TGA silver to join 5mL 1-(6 '-hydroxyl) hexyl-3-methyl imidazolium tetrafluoroborate ([C
6OHmim] BF
4) in the ionic liquid, ultrasonicly making its dispersion, constant temperature is 6 hours in 160 ℃ of oil baths, the centrifugation of cool to room temperature afterproduct, with distilled water washing four times, last normal temperature vacuum drying.Promptly get the Ag nano wire.The Ag wire diameter distribution broad that makes is distributed between the 40-100nm, and length surpasses 5 μ m.
Embodiment 4 preparation Pd nanometer rods
(1) ion liquid preparation: 1-(6 '-hydroxyl) hexyl-3-methyl imidazolium tetrafluoroborate ([C
6OHmim] BF
4) ion liquid preparation process is with embodiment 1;
(2) claim 5mg PdCl
2Be dissolved in 3mL 1-(6 '-hydroxyl) hexyl-3-methyl imidazolium tetrafluoroborate ([C
6OHmim] BF
4) in the ionic liquid, ultrasonicly making its dispersion, constant temperature is 4 hours in 160 ℃ of oil baths, the centrifugation of cool to room temperature afterproduct, with distilled water washing four times, last normal temperature vacuum drying.Promptly get the Pd nanometer rods.The Pd nanometer rods that obtains is acicular texture.Length is between 1～2 μ m.
Embodiment 5 preparation Ag nanoparticles
(1) ion liquid preparation: 1-ethoxy-3-methyl imidazolium tetrafluoroborate ([C
2OHmim] BF
4) ion liquid preparation process is with embodiment 1;
(2) with 1mg AgBF
4Join 5mL 1-ethoxy-3-methyl imidazolium tetrafluoroborate ([C
2OHmim] BF
4) in the ionic liquid, ultrasonic processing makes its dissolving, stop heating after 8 hours in heating in 80 ℃ of oil baths, with the product centrifugation, wash four times vacuum drying under the normal temperature then with acetone after the cooling, promptly obtain the Ag nanoparticle, average grain diameter is 50nm, but the particle diameter distribution is more inhomogeneous, is the face-centered cubic crystal formation.
Embodiment 6 preparation Ag nanoparticles
(1) ion liquid preparation: N-ethoxy pyridine ion liquid preparation process is with embodiment 1;
(2) with 10mg AgBF
4Join in the 5mL N-ethoxy pyridine ion liquid, ultrasonic processing makes its dissolving, stop heating after 0.5 hour in heating in 200 ℃ of oil baths, with the product centrifugation, wash four times vacuum drying under the normal temperature then with acetone after the cooling, promptly obtain the Ag nanoparticle, average grain diameter is that particle diameter is evenly distributed about 40nm, is the face-centered cubic crystal formation.
Claims (5)
1, the hydroxy ion liquid reduction prepares the method for metal nanoparticle, it is characterized in that, comprises following step:
(1) makes ionic liquid by cation and a kind of acid radical anion of hydroxy functional groups on a kind of side chain;
(2) metal oxide, metal hydroxides or slaine are dispersed or dissolved in the ionic liquid through ultrasonic;
(3) liquid-phase reaction system that will disperse or dissolve heats under oil bath;
(4) product separates in the system of back to reacting, and separated products is washed and vacuum drying treatment.
2, by the described method for preparing metal nanoparticle of claim 1, it is characterized in that the cation of hydroxy functional groups is N-hydroxyalkyl pyridinium ion, N-hydroxyalkyl-N-alkyl imidazole ion or N, N-dihydroxyalkyl imidazol ion on the side chain; Anion is F
-, Cl
-, Br
-, BF
4 -, PF
6 -, NO
3 -, CF
3COO
-, C
3F
7COO
-, CF
3SO
3 -, C
4F
9SO
3 -, (CF
3SO
2)
2N
-, (C
2F
5SO
2)
2N
-, (CF
3SO
2)
3C
-, SbF
6 -, AsF
6 -
3, by the described method for preparing metal nanoparticle of claim 2, it is characterized in that glyoxaline cation is:
Wherein k is the integer of 0-11, and m is the integer of 0-9, and n is the integer of 0-9;
Pyridylium is:
Wherein n is the integer of 0-9;
Metal oxide, metal hydroxides or slaine are IB, IIB except that Zn, Fe, Co compound, solid metal oxide, metal hydroxides or the slaine of VIIIB.
4, by the described method for preparing metal nanoparticle of claim 3, it is characterized in that slaine is sulfate, carbonate, nitrate, oxalates, acetate, iodate, borofluoride, fluorophosphate or halide.
5, by claim 1,2, the 3 or 4 described methods that prepare metal nanoparticle, it is characterized in that be 0.5-8h described heat time heating time, described heating-up temperature is 80 ℃-200 ℃.
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| CN100496819C CN100496819C (en) | 2009-06-10 |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102369154A (en) * | 2009-04-08 | 2012-03-07 | 徐光锡 | Production method for a metal nanostructure using an ionic liquid |
| CN102672195A (en) * | 2012-01-04 | 2012-09-19 | 河南科技大学 | Preparation method of gold nanoparticles |
| CN103864692A (en) * | 2012-12-07 | 2014-06-18 | 财团法人工业技术研究院 | Ionic liquid and method for extracting grease by using ionic liquid |
| CN103958097A (en) * | 2011-09-30 | 2014-07-30 | 劳伦斯·T·德扎尔 | Method of preparing metal nanoparticles |
| CN109550974A (en) * | 2018-12-13 | 2019-04-02 | 华南理工大学 | A kind of preparation method using carnosic acid green syt nano silver |
| CN110560158A (en) * | 2019-08-30 | 2019-12-13 | 浙江工业大学 | High-dispersion supported ionic liquid-palladium aluminum oxide catalyst and preparation method and application thereof |
| CN111167439A (en) * | 2020-01-16 | 2020-05-19 | 河南科技大学 | Chrysanthemum-shaped Pd nano particle |
| CN111618311A (en) * | 2019-02-28 | 2020-09-04 | 中国科学院化学研究所 | Silver nanoparticle dispersion liquid and preparation method and application thereof |
| CN111701618A (en) * | 2020-06-28 | 2020-09-25 | 江苏思派新能源科技有限公司 | Ionic liquid catalyst and preparation method and application thereof |
| CN113414401A (en) * | 2021-06-22 | 2021-09-21 | 山东建邦胶体材料有限公司 | Silver powder of crystalline silicon solar PERC battery silver paste and preparation method thereof |
-
2005
- 2005-10-18 CN CNB2005100484157A patent/CN100496819C/en not_active Expired - Fee Related
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102369154B (en) * | 2009-04-08 | 2015-02-18 | 徐光锡 | Production method for a metal nanostructure using an ionic liquid |
| CN102369154A (en) * | 2009-04-08 | 2012-03-07 | 徐光锡 | Production method for a metal nanostructure using an ionic liquid |
| CN103958097A (en) * | 2011-09-30 | 2014-07-30 | 劳伦斯·T·德扎尔 | Method of preparing metal nanoparticles |
| CN102672195A (en) * | 2012-01-04 | 2012-09-19 | 河南科技大学 | Preparation method of gold nanoparticles |
| CN102672195B (en) * | 2012-01-04 | 2013-11-27 | 河南科技大学 | Preparation method of gold nanoparticles |
| CN103864692B (en) * | 2012-12-07 | 2015-07-08 | 财团法人工业技术研究院 | Ionic liquid and method for extracting grease by using ionic liquid |
| CN103864692A (en) * | 2012-12-07 | 2014-06-18 | 财团法人工业技术研究院 | Ionic liquid and method for extracting grease by using ionic liquid |
| CN109550974A (en) * | 2018-12-13 | 2019-04-02 | 华南理工大学 | A kind of preparation method using carnosic acid green syt nano silver |
| CN111618311A (en) * | 2019-02-28 | 2020-09-04 | 中国科学院化学研究所 | Silver nanoparticle dispersion liquid and preparation method and application thereof |
| CN110560158A (en) * | 2019-08-30 | 2019-12-13 | 浙江工业大学 | High-dispersion supported ionic liquid-palladium aluminum oxide catalyst and preparation method and application thereof |
| CN111167439A (en) * | 2020-01-16 | 2020-05-19 | 河南科技大学 | Chrysanthemum-shaped Pd nano particle |
| CN111701618A (en) * | 2020-06-28 | 2020-09-25 | 江苏思派新能源科技有限公司 | Ionic liquid catalyst and preparation method and application thereof |
| CN113414401A (en) * | 2021-06-22 | 2021-09-21 | 山东建邦胶体材料有限公司 | Silver powder of crystalline silicon solar PERC battery silver paste and preparation method thereof |
| CN113414401B (en) * | 2021-06-22 | 2022-03-15 | 山东建邦胶体材料有限公司 | Silver powder of crystalline silicon solar PERC battery silver paste and preparation method thereof |
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|---|---|
| CN100496819C (en) | 2009-06-10 |
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